|
Kacelnik, A. (1990). R.C. Bolies and M.D. Beecher, Editors, Evolution and Learning, Lawrence Erlbaum, Hillsdale, New Jersey (1988), p. x. Anim. Behav., 40(3), 602–603.
|
|
Cheney DL, & Seyfarth RM. (1990). Attending to behaviour versus attending to knowledge: examining monkeys' attribution of mental states. Anim. Behav., 40, 742.
|
Thouless, C. R. (1990). Feeding competition between grazing red deer hinds. Anim. Behav., 40(1), 105–111.
Abstract: The effect of social rank on the feeding behaviour of female red deer, Cervus elaphus L., on the Isle of Rhum, Scotland, was investigated. Hinds were less likely to approach and more likely to leave the vicinity of other individuals if these hinds were dominant to them. Movements away by subordinates were more likely to involve a break from feeding. Feeding rate, as measured by bite rate, increased with distance from dominant neighbours, but was unaffected by the distance to subordinates. It appears that aggressive interactions had little direct effect on access to food. Instead, it is suggested that feeding competition in red deer hinds is largely a passive process, operating through the avoidance of conflict by subordinates.
|
Beauchamp, G., & Kacelnik, A. (1991). Effects of the knowledge of partners on learning rates in zebra finches Taeniopygia guttata. Anim. Behav., 41(2), 247–253.
Abstract: Many interpretations of the adaptive value of group living involve tranfer of knowledge. However, according to learning theory, being in a pair with a knowledgeable partner can have paradoxical consequences. Obtaining food by following a skilled companion may reduce the ability of naive individuals to learn about clues that signal the occurrence of food. This study examined the relation between learning and following in paris of zebra finches. Knowledgeable partners were trained to obtain food from a computer-controlled dispenser by using the information provided by a signal. For non-knowledgeable partners, the signal was irrelevant and could not be used to predict foraging opportunities. The rate of learning about the signal by naive birds that shared the experience of either knowledgeable or nonknowledgeable tutors was then examined. Naive birds learned more slowly as a result of being in a pair with a knowledgeable than a non-knowledgeable partner. Well-informed mates acted as a reliable cue to predict foraging opportunities, and thus overshadowed the independent signal. The knowledge of a partner influences learning rates in naive individuals, but in the opposite direction to that predicted by earlier accounts of learning in social contexts.
|
Chapais, B., Girard, M., & Primi, G. (1991). Non-kin alliances, and the stability of matrilineal dominance relations in Japanese macaques. Anim. Behav., 41(3), 481–491.
Abstract: Alliances among kin play a major role in a female's acquisition of her mother's dominance rank in many species of cercopithecines. It is noteworthy, however, that kin rarely form coalitions to challenge females from higher-ranking matrilines, and that matrilineal hierarchies are remarkably stable. One possible reason for the rarity of destabilizing coalitions is that members of high-ranking matrilines form alliances against lower ranking ones. In this paper the patterning of aggressive support among non-kin, and its effect on the stability of rank relations are analysed in a captive group of Japanese macaques, Macaca fuscata, composed of three unrelated matrilines. Analysis of the distribution of non-kin interventions in conflicts between matrilines over a 52-month period revealed a clear pattern of preferential support between the two dominant matrilines against the third-ranking one. This pattern was confirmed experimentally. Any member of the two dominant matrilines was unable, individually, to maintain its rank above the third-ranking matriline, but was able to do so in the presence of the other dominant matriline. Non-kin alliances appear to prevent subordinate females from challenging higher ranking females through revolutionary coalitions (formed among subordinates) or through bridging coalitions (formed among individuals ranking above and below the target). Non-kin support is interpreted in terms of cooperation versus reciprocal altruism.
|
|
Boesch, C. (1991). Teaching among wild chimpanzees. Anim. Behav., 41(3), 530–532.
|
Kacelnik, A., & Todd, I. A. (1992). Psychological mechanisms and the Marginal Value Theorem: effect of variability in travel time on patch exploitation. Anim. Behav., 43(2), 313–322.
Abstract: The Marginal Value Theorem (MVT) describes the behaviour that maximizes the ratio of expected gain over expected foraging time in a patchy environment. When travel time is variable, the MVT rationale and its predictions are sensitive only to the mean travel time and not to the spread or skew of the distribution. Two mechanistic arguments contradict these predictions. First, tests of the MVT have previously shown that there is a disproportionate influence of the last travel time, and second, psychological models of information processing suggest that memory for time intervals is strongly dependent on the scatter of the distribution experienced. These mechanistic concepts, combined with Jensen's inequality, suggest that patch exploitation should decrease as the scatter of the travel distribution increases. In a Skinner box experiment with pigeons, Columba livia, the problem was examined by simulating three environments with identical patches and the same mean travel time, but different travel time variability. Patch exploitation decreased with increasing variance in travel time. The results are used to argue in favour of the inclusion of realistic psychological properties as constraints in functional models of behaviour. Although both the MVT and the mechanistic models account for some features of the results, none of them can explain all the findings.
|
|
Povinelli DJ, Nelson KE, & Boysen ST. (1992). Comprehension of role reversal in chimpanzees: evidence of empathy? Anim. Behav., 43, 633.
|
Brunner, D., Kacelnik, A., & Gibbon, J. (1992). Optimal foraging and timing processes in the starling, Sturnus vulgaris: effect of inter-capture interval. Anim. Behav., 44(4), 597–613.
Abstract: Laboratory experiments with starlings, Sturnus vulgaris, were conducted to investigate the interaction between timing and cost-benefit considerations. The design simulated an environment in which food was distributed in patches. Patches contained a random number of food items (N=0-4) separated by a fixed inter-capture interval or fixed interval. All patches ended with sudden depletion. The time elapsed since the last prey capture was the only way to detect the depletion of the patch. Once the patch was depleted a new patch could be reached by travelling between two perches. Three measures of timing were taken: (1) rate of working for food as function of `waiting' time in a patch, (2) the time of the last response in a patch or `giving-in' time, and (3) the time at which travel was initiated or `moving-on' time. The fixed interval that characterized patches was varied between conditions. The mean time of the peak in working rate was consistently centred around the fixed interval, while the other two measures of timing kept a roughly linear relation to the fixed interval, with slope greater than one. In accordance with Scalar Expectancy Theory, variability in the three forms of timing was proportional to the magnitude of the fixed interval. The birds seemed to take account of this increase in variability as shown by the mean value of their giving-up criterion. These results imply that information-processing constraints are important for modelling behavioural optimality.
|
Caraco, T., Kacelnik, A., Mesnick, N., & Smulewitz, M. (1992). Short-term rate maximization when rewards and delays covary. Anim. Behav., 44(Part 3), 441–447.
Abstract: In nature foragers must exploit resources that vary randomly in both the energy acquired per item (reward) and the time required to pursue, capture and process an item (delay). Furthermore, rewards and delays associated with particular resources may often covary significantly. An analytical model asks how variance-covariance levels for rewards and delays could influence choice of resources when lack of information or cognitive limitation implies that a consumer attempts to maximize its short-term rate of energy gain. Both greater expected reward and reduced expected delay clearly should enhance preference for a resource. The model predicts that increased delay variance and reduced reward-delay covariance should increase a forager's preference for a resource. A forager should be risk-averse towards reward variance when the reward-delay covariance is positive, but should become risk-prone towards reward variance when the reward-delay covariance is negative.
|
